438 research outputs found

    Finite-Difference and Pseudo-Sprectral Methods for the Numerical Simulations of In Vitro Human Tumor Cell Population Kinetics

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    Pseudo-spectral approximations are constructed for the model equations which describe the population kinetics of human tumor cells in vitro and their responses to radiotherapy or chemotherapy. These approximations are more efficient than finite-difference approximations. The spectral accuracy of the pseudo-spectral method allows us to resolve the model with a much smaller number of spatial grid-points than required for the finite-difference method to achieve comparable accuracy. This is demonstrated by numerical experiments which show a good agreement between predicted and experimental data

    Multi-dimensional parameter estimation of heavy-tailed moving averages

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    In this paper we present a parametric estimation method for certain multi-parameter heavy-tailed L\'evy-driven moving averages. The theory relies on recent multivariate central limit theorems obtained in [3] via Malliavin calculus on Poisson spaces. Our minimal contrast approach is related to the papers [14, 15], which propose to use the marginal empirical characteristic function to estimate the one-dimensional parameter of the kernel function and the stability index of the driving L\'evy motion. We extend their work to allow for a multi-parametric framework that in particular includes the important examples of the linear fractional stable motion, the stable Ornstein-Uhlenbeck process, certain CARMA(2, 1) models and Ornstein-Uhlenbeck processes with a periodic component among other models. We present both the consistency and the associated central limit theorem of the minimal contrast estimator. Furthermore, we demonstrate numerical analysis to uncover the finite sample performance of our method

    An siRNA-based method for efficient silencing of gene expression in mature brown adipocytes

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    Brown adipose tissue is a promising therapeutic target for opposing obesity, glucose intolerance and insulin resistance. The ability to modulate gene expression in mature brown adipocytes is important to understand brown adipocyte function and delineate novel regulatory mechanisms of non-shivering thermogenesis. The aim of this study was to optimize a lipofection-based small interfering RNA (siRNA) transfection protocol for efficient silencing of gene expression in mature brown adipocytes. We determined that a critical parameter was to deliver the siRNA to mature adipocytes by reverse transfection, i.e. transfection of non-adherent cells. Using this protocol, we effectively knocked down both high- and low-abundance transcripts in a model of mature brown adipocytes (WT-1) as well as in primary mature mouse brown adipocytes. A functional consequence of the knockdown was confirmed by an attenuated increase in uncoupled respiration (thermogenesis) in response to β-adrenergic stimulation of mature WT-1 brown adipocytes transfected with uncoupling protein 1 siRNA. Efficient gene silencing was also obtained in various mouse and human white adipocyte models (3T3-L1, primary mouse white adipocytes, hMADS) with the ability to undergo “browning.” In summary, we report an easy and versatile reverse siRNA transfection protocol to achieve specific silencing of gene expression in various models of mature brown and browning-competent white adipocytes, including primary cells

    Regulation of glycolysis in brown adipocytes by HIF-1α

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    Brown adipose tissue takes up large amounts of glucose during cold exposure in mice and humans. Here we report an induction of glucose transporter 1 expression and increased expression of several glycolytic enzymes in brown adipose tissue from cold-exposed mice. Accordingly, these genes were also induced after β-adrenergic activation of cultured brown adipocytes, concomitant with accumulation of hypoxia inducible factor-1α (HIF-1α) protein levels. HIF-1α accumulation was dependent on uncoupling protein 1 and generation of mitochondrial reactive oxygen species. Expression of key glycolytic enzymes was reduced after knockdown of HIF-1α in mature brown adipocytes. Glucose consumption, lactate export and glycolytic capacity were reduced in brown adipocytes depleted of Hif-1α. Finally, we observed a decreased β-adrenergically induced oxygen consumption in Hif-1α knockdown adipocytes cultured in medium with glucose as the only exogenously added fuel. These data suggest that HIF-1α-dependent regulation of glycolysis is necessary for maximum glucose metabolism in brown adipocytes.ISSN:2045-232

    Cell cycle times of short-term cultures of brain cancers as predictors of survival

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    Tumour cytokinetics estimated in vivo as potential doubling times (Tpot values) have been found to range in a variety of human cancers from 2 days to several weeks and are often related to clinical outcome. We have previously developed a method to estimate culture cycle times of short-term cultures of surgical material for several tumour types and found, surprisingly, that their range was similar to that reported for Tpot values. As Tpot is recognised as important prognostic variable in cancer, we wished to determine whether culture cycle times had clinical significance. Brain tumour material obtained at surgery from 70 patients with glioblastoma, medulloblastoma, astrocytoma, oligodendroglioma and metastatic melanoma was cultured for 7 days on 96-well plates, coated with agarose to prevent proliferation of fibroblasts. Culture cycle times were estimated from relative 3H-thymidine incorporation in the presence and absence of cell division. Patients were divided into two groups on the basis of culture cycle times of ⩽10 days and >10 days and patient survival was compared. For patients with brain cancers of all types, median survival for the ⩽10-day and >10-day groups were 5.1 and 12.5 months, respectively (P=0.0009). For 42 patients with glioblastoma, the corresponding values were 6.5 and 9.0 months, respectively (P=0.03). Lower grade gliomas had longer median culture cycle times (16 days) than those of medulloblastomas (9.9 days), glioblastomas (9.8 days) or melanomas (6.7 days). We conclude that culture cycle times determined using short-term cultures of surgical material from brain tumours correlate with patient survival. Tumour cells thus appear to preserve important cytokinetic characteristics when transferred to culture

    Global gene expression profiling of brown to white adipose tissue transformation in sheep reveals novel transcriptional components linked to adipose remodeling

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    BACKGROUND: Large mammals are capable of thermoregulation shortly after birth due to the presence of brown adipose tissue (BAT). The majority of BAT disappears after birth and is replaced by white adipose tissue (WAT). RESULTS: We analyzed the postnatal transformation of adipose in sheep with a time course study of the perirenal adipose depot. We observed changes in tissue morphology, gene expression and metabolism within the first two weeks of postnatal life consistent with the expected transition from BAT to WAT. The transformation was characterized by massively decreased mitochondrial abundance and down-regulation of gene expression related to mitochondrial function and oxidative phosphorylation. Global gene expression profiling demonstrated that the time points grouped into three phases: a brown adipose phase, a transition phase and a white adipose phase. Between the brown adipose and the transition phase 170 genes were differentially expressed, and 717 genes were differentially expressed between the transition and the white adipose phase. Thirty-eight genes were shared among the two sets of differentially expressed genes. We identified a number of regulated transcription factors, including NR1H3, MYC, KLF4, ESR1, RELA and BCL6, which were linked to the overall changes in gene expression during the adipose tissue remodeling. Finally, the perirenal adipose tissue expressed both brown and brite/beige adipocyte marker genes at birth, the expression of which changed substantially over time. CONCLUSIONS: Using global gene expression profiling of the postnatal BAT to WAT transformation in sheep, we provide novel insight into adipose tissue plasticity in a large mammal, including identification of novel transcriptional components linked to adipose tissue remodeling. Moreover, our data set provides a useful resource for further studies in adipose tissue plasticity. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1405-8) contains supplementary material, which is available to authorized users

    Retinoic acid has different effects on UCP1 expression in mouse and human adipocytes

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    BACKGROUND: Increased adipose thermogenesis is being considered as a strategy aimed at preventing or reversing obesity. Thus, regulation of the uncoupling protein 1 (UCP1) gene in human adipocytes is of significant interest. Retinoic acid (RA), the carboxylic acid form of vitamin A, displays agonist activity toward several nuclear hormone receptors, including RA receptors (RARs) and peroxisome proliferator-activated receptor δ (PPARδ). Moreover, RA is a potent positive regulator of UCP1 expression in mouse adipocytes. RESULTS: The effects of all-trans RA (ATRA) on UCP1 gene expression in models of mouse and human adipocyte differentiation were investigated. ATRA induced UCP1 expression in all mouse white and brown adipocytes, but inhibited or had no effect on UCP1 expression in human adipocyte cell lines and primary human white adipocytes. Experiments with various RAR agonists and a RAR antagonist in mouse cells demonstrated that the stimulatory effect of ATRA on UCP1 gene expression was indeed mediated by RARs. Consistently, a PPARδ agonist was without effect. Moreover, the ATRA-mediated induction of UCP1 expression in mouse adipocytes was independent of PPARγ coactivator-1α. CONCLUSIONS: UCP1 expression is differently affected by ATRA in mouse and human adipocytes. ATRA induces UCP1 expression in mouse adipocytes through activation of RARs, whereas expression of UCP1 in human adipocytes is not increased by exposure to ATRA

    Modelling radiation-induced cell cycle delays

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    Ionizing radiation is known to delay the cell cycle progression. In particular after particle exposure significant delays have been observed and it has been shown that the extent of delay affects the expression of damage such as chromosome aberrations. Thus, to predict how cells respond to ionizing radiation and to derive reliable estimates of radiation risks, information about radiation-induced cell cycle perturbations is required. In the present study we describe and apply a method for retrieval of information about the time-course of all cell cycle phases from experimental data on the mitotic index only. We study the progression of mammalian cells through the cell cycle after exposure. The analysis reveals a prolonged block of damaged cells in the G2 phase. Furthermore, by performing an error analysis on simulated data valuable information for the design of experimental studies has been obtained. The analysis showed that the number of cells analyzed in an experimental sample should be at least 100 to obtain a relative error less than 20%.Comment: 19 pages, 11 figures, accepted for publication in Radiation and Environmental Biophysic

    STRATEGI PENINGKATAN KESADARAN DAN KEPEDULIAN TERHADAP EKOSISTEM MANGROVE PADA MURID SDN 54 DAN SDN 206 DI KELURAHAN PALLAMEANG, KECAMATAN MATTIRO SOMPE, KABUPATEN PINRANG: Strategy to Increase Awareness and Concern on Mangrove Ecosystem to the Students of SDN 54 and SDN 206 in Pallameang Village, Mattiro Sompe District, Pinrang Regency

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    Ekosistem mangrove merupakan salah satu ekosistem yang memiliki fungsi ekologis dan ekonomis yang penting bagi masyarakat. Kelurahan Pallameang, Kecamatan Mattiro Sompe, Kabupaten Pinrang, saat ini mengalami abrasi secara terus menerus pada daerah pesisir pantai. Hal ini dikarenakan kawasan tersebut telah kehilangan mangrove yang merupakan salah satu pelindung alami pesisir pantai. Kesadaran untuk menjaga lingkungan sebagai tempat bermukim dan sumber kehidupan masyarakat membutuhkan proses yang harus dimulai sejak usia muda. Kegiatan Pengabdian kepada Masyarakat ini dilaksanakan pada murid Kelas V SDN 54 dan SDN 206 di Kelurahan Pallameang dengan menggunakan metode pengajaran aktif-demonstratif. Tahapan kegiatan yang dilakukan meliputi penyampaian materi tentang ekosistem mangrove, jenis-jenis mangrove, biota yang berasosiasi dengan mangrove, kemudian dilanjutkan dengan demonstrasi pengenalan beberapa jenis mangrove. Selain itu, juga dilakukan pre-test dan post-test, lomba membaca, dan lomba menggambar jenis-jenis mangrove. Hasil dari kegiatan ini menunjukkan bahwa anak usia dini di Kelurahan Pallameang membutuhkan bentuk pembelajaran muatan lokal mengenai pengenalan lingkungan ekosistem mangrove. Hal ini terlihat dari kurangnya pengetahuan siswa tentang peran ekosistem mangrove bagi lingkungan, namun minat dan antusias siswa sangat tinggi dalam mengikuti kegiatan pengenalan ekosistem mangrove ini. Kata kunci: Murid kelas V SD, Mangrove, Kelurahan Pallameang, Kecamatan Mattiro Sompe, Kabupaten Pinrang.                                                                  ABSTRACT Mangrove ecosystem is an ecosystem with an ecology and economic benefit for coastal livelihood. The Pallameang Village of Mattiro Sompe District in Pinrang Regency, is currently experiencing continuous abrasion of its coastal area. This is because the area has lost mangroves as the natural protectors of the coast. The awareness to protect the mangrove ecosystem as resources where this coastal community depends on for their livelihood requires a process that must be started at a young age. Our community services were carried out for the 5th grade class students at SDN 54 and SDN 206 in Pallameang Village by active-demonstrative teaching method. The activities carried out through: 1) slides presentation on mangrove ecosystem, mangrove species, associated biota of mangrove, 2) introducing mangroves species found in the area, and 3) competitions on reading and drawing related to mangrove. In addition, we conduct pre-test and post-test. The results of the test indicate that children in Pallameang Village require a form of local content learning in regard to mangrove ecosystem in their area. These students have no knowledge on the role of mangrove ecosystems for the environment Nevertheless, the interest and enthusiasm of students were very high in participating in all activities of our community service in the introduction of mangrove ecosystem. Keywords: Fifth grade elementary school students, Mangroves, Pallameang Village, Mattiro Sompe District, Pinrang Regency

    Role of IL-6 in Exercise Training- and Cold-Induced UCP1 Expression in Subcutaneous White Adipose Tissue

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    Expression of brown adipose tissue (BAT) associated proteins like uncoupling protein 1 (UCP1) in inguinal WAT (iWAT) has been suggested to alter iWAT metabolism. The aim of this study was to investigate the role of interleukin-6 (IL-6) in exercise training and cold exposure-induced iWAT UCP1 expression. The effect of daily intraperitoneal injections of IL-6 (3 ng/g) in C57BL/6 mice for 7 days on iWAT UCP1 expression was examined. In addition, the expression of UCP1 in iWAT was determined in response to 3 days of cold exposure (4°C) and 5 weeks of exercise training in wild type (WT) and whole body IL-6 knockout (KO) mice. Repeated injections of IL-6 in C57BL/6 mice increased UCP1 mRNA but not UCP1 protein content in iWAT. Cold exposure increased iWAT UCP1 mRNA content similarly in IL-6 KO and WT mice, while exercise training increased iWAT UCP1 mRNA in WT mice but not in IL-6 KO mice. Additionally, a cold exposure-induced increase in iWAT UCP1 protein content was blunted in IL-6 KO mice, while UCP1 protein content in iWAT was lower in both untrained and exercise trained IL-6 KO mice than in WT mice. In conclusion, repeated daily increases in plasma IL-6 can increase iWAT UCP1 mRNA content and IL-6 is required for an exercise training-induced increase in iWAT UCP1 mRNA content. In addition IL-6 is required for a full induction of UCP1 protein expression in response to cold exposure and influences the UCP1 protein content iWAT of both untrained and exercise trained animals
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